Odocoileus virginianus Quercus virginiana) maritime …...impact deer management decisions, my...
Transcript of Odocoileus virginianus Quercus virginiana) maritime …...impact deer management decisions, my...
ABSTRACT
SHERRILL, BRANDON LEE. Assessment of White-tailed Deer on Bald Head Island, North
Carolina. (Under the direction of Christopher S. DePerno).
In recent years, the white-tailed deer (Odocoileus virginianus) population on Bald Head
Island, North Carolina has increased. Bald Head Island is ~620 ha and is characterized by
live oak (Quercus virginiana) maritime forest, dunes, tidal marsh, and urban development.
Maritime forests are unique and important coastal habitats that are under significant threat
from development, and in the absence of reproductive controls, white-tailed deer can
negatively impact ecosystems through over-browsing. Preservation of maritime forest is
important for barrier island conservation. Therefore, to provide empirical data that could
impact deer management decisions, my objectives were to determine emigration, home
range, cover type use, and population density of white-tailed deer on Bald Head Island.
From 5 January through 31 March 2008 and 2 January through 31 January 2009, 12 females
and one male were chemically immobilized and equipped with VHF radiocollars. From
January 2008 through January 2010, a minimum of four visual locations were obtained per
animal per month. We used a fixed kernel density estimator to calculate 90% (home range)
and 50% (core area) utilization contours for radiocollared female deer (n = 11). To
determine cover type use and selection, I used land cover data generated by the Southeast
Gap Analysis Project and a Chi-square ( 2) goodness-of fit test to determine differences
between expected and observed use of cover types within home ranges. Significance levels
for 95% confidence intervals were determined using the Bonferroni method. From May
through August 2008 and 2009, spotlight surveys were conducted and used to generate
population estimates with a Lincoln-Peterson index. No radiocollared white-tailed deer
migrated from Bald Head Island during the course of the study and average home range and
core areas were 60.73 ha (SE = 5.63) and 15.00 ha (SE = 1.37), respectively. Maritime
forest/shrub comprised ~275 ha (44%) of available habitat on Bald Head Island and were
used by radiocollared deer at levels greater than available, whereas dune/grasslands were
used less than available. All other cover types were used in proportion to availability.
Population densities of white-tailed deer were 17 and 15 deer/km2 for 2008 and 2009,
respectively. Based on home range size and cover type selection and until additional
research is conducted, I recommend that white-tailed deer populations be managed at current
levels to prevent degradation of this important maritime forest ecosystem.
Additionally, white-tailed deer were screened for multiple pathogens to provide
baseline data on exposure to zoonotic diseases. Blood was collected from eight deer in
January through March 2008 and five deer in January 2009. Serum samples were tested for
antibodies to Anaplasma phagocytophilum, Borrelia burgdorferi, and six serovars of
Leptospira interrogans, and whole blood samples for DNA from Bartonella spp. and B.
burgdorferi. Serum samples were screened using a polyvalent enzyme-linked
immunosorbent assay (ELISA), an indirect fluorescent antibody (IFA) test, or a microscopic
agglutination test (MAT). Whole blood samples were screened using conventional
polymerase chain reaction (PCR) analysis. All sera were negative for L. interrogans, two
serum samples tested positive for A. phagocytophilum, and one was positive for B.
burgdorferi. Whole blood PCR results were negative for Bartonella spp. and B. burgdorferi.
Continued surveillance of wildlife disease is necessary to determine prevalence of specific
pathogens, their impacts on the white-tailed deer population, and the risk of human exposure.
Assessment of White-tailed Deer on Bald Head Island, North Carolina
by
Brandon Lee Sherrill
A thesis submitted to the Graduate Faculty of
North Carolina State University
in partial fulfillment of the
requirements for the Degree of
Master of Science
Fisheries, Wildlife, and Conservation Biology
Raleigh, North Carolina
2010
APPROVED BY:
_______________________________ ______________________________
Christopher S. DePerno Suzanne Kennedy-Stoskopf
Chair of Advisory Committee
________________________________
Heather M. Cheshire
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DEDICATION
I dedicate my thesis to my Mom and Dad, for their love and support throughout my
education; to all my siblings; and especially to Jessie Birckhead, for being a constant source
of encouragement and always being willing to listen.
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BIOGRAPHY
Brandon Lee Sherrill was born in Statesville, North Carolina on December 10, 1981 to
parents Ted and Deborah Sherrill. He has a twin brother, Bryan, younger brother, Chris, and
a younger sister, Lauren. Brandon grew up spending much of his free time outdoors,
exploring the woods outside his home. He enjoyed fishing, hiking, and photographing
nature. After graduating from South Iredell High School in 2000, Brandon spent several
years deciding what path he should pursue at the collegiate level. He eventually determined
his love of wildlife and the outdoors was leading him to a career in the sciences; preferably
dealing with wildlife research and management. He graduated with a Bachelor degree in
Fisheries and Wildlife Sciences in 2006 from North Carolina State University. After
graduation, Brandon worked as a research technician for North Carolina State University at
the Hill Demonstration Forest where he further developed his skills in wildlife research.
After several years of working as a research technician, and in other jobs not related to
wildlife, Brandon decided to return to school to earn a Master‟s degree to allow him more
opportunities in the field of wildlife research and management. He began his graduate career
at North Carolina State University in the Fisheries, Wildlife, and Conservation Biology
Program in January 2008. Upon graduation, Brandon would like to pursue a career in
wildlife management in a state or federal agency.
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ACKNOWLEDGMENTS
This research was funded by the Village of Bald Head Island, North Carolina State
University‟s Department of Forestry and Environmental Resources, Fisheries, Wildlife, and
Conservation Biology Program, and the University of North Carolina at Wilmington‟s
Department of Environmental Science. I thank Dr. Chris S. DePerno, Dr. Anthony C.
Snider, Dr. Suzanne Kennedy-Stoskopf, and Dr. Heather M. Cheshire for their assistance in
the field and with data analysis during this project. A special thanks to Paula Gillikin for her
guidance and expertise while collecting our sample of white-tailed deer (and also to
Lookout). Dr. Michael Stoskopf and Dr. Sathya Chinnadurai were vital during our initial
sampling period, both in the field and via email, by answering numerous questions regarding
immobilizing drugs. I thank Dr. John Taggart for his assistance characterizing vegetative
communities on Bald Head Island.
A special thanks to all of the undergraduate and graduate students that helped out in
field during data collection. The following students helped with the chemical immobilization
of white-tailed deer or with collection of telemetry locations: Andy Almeter, Jessie
Birckhead, Colter Chitwood, Jimmy Dodson, Lauren Fields, John Henry Harrelson, Doug
Noonan, Mike Nunnery, Liz Rivers, and numerous students from UNCW‟s research
techniques course. In addition, I would like to extend my gratitude to the Bald Head Island
Conservancy for their constant support of our project through the supply of golf carts,
spotlights, and housing. Maureen Dewire, Dr. Suzanne Dorsey, Brett DeGregorio (and
especially Nico), and Dr. Thomas Hancock were all very helpful during my stays in the
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dormitory. Also, I thank the interns at the conservancy who conducted numerous spotlight
surveys of white-tailed deer.
There are multiple residents of Bald Head Island that deserve mention for their
contributions to the project. Thanks to the George and Martha Hayworth, Doug and Jane
Oakley, and James and Margaret Leutze for allowing our team of researchers to use their
homes for extended periods of time. Also, I would like to extend a very special thanks to the
late Anne Pickering for her enduring support and for the delicious food she provided at the
end of some of our long, cold nights in the field.
I thank Cindy Burke for all of her hard work and for her kind spirit in the office. As
our program secretary, Cindy was always there to help sort out paperwork, provide guidance,
and was always willing to listen to all my stories and problems. Also, I would like to thank
all of the faculty and graduate students at the Turner House for all the wonderful years in
North Carolina State University‟s Fisheries, Wildlife, and Conservation Biology Program.
Finally, I would like to thank my family and friends for all their support in my
educational career. Daddy, thanks for always being there to talk to and to answer questions I
couldn‟t figure out on my own, and especially for the financial support when the graduate
stipend just wasn‟t enough to get me through the month. Mama, thanks for all your love, and
for always being concerned for my well-being. To all my siblings, thanks for being around
and hanging out when I could make it back home, as infrequent as it may have been. Colter,
thanks for being my “brother” in the office and for being my hunting companion in the
woods. Of course, I can‟t thank Colter without mentioning John Henry. John, thanks for all
the years of swapping stories (hunting related and otherwise) and for being a good friend.
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Most importantly, I want to thank Jessie for all your love and support. Graduate school
would have been much less manageable without having you to listen to all of my stories
regarding field work, teaching, and just the everyday events that make up the life of a
graduate student.
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TABLE OF CONTENTS
LIST OF TABLES viii
ASSESSMENT OF WHITE-TAILED DEER ON
BALD HEAD ISLAND, NORTH CAROLINA 1
Introduction 1
WHITE-TAILED DEER ON A BARRIER ISLAND: IMPLICATIONS FOR
PRESERVING AN ECOLOGICALLY IMPORTANT MARITIME FOREST 3
Abstract 3
Introduction 4
Study Area 7
Methods 8
Results 11
Discussion 12
Management Implications 15
Acknowledgments 16
Literature Cited 17
SURVEY OF ZOONOTIC PATHOGENS IN WHITE-TAILED
DEER ON BALD HEAD ISLAND, NORTH CAROLINA 24
Abstract 24
Literature Cited 28
CONCLUSIONS 30
APPENDICES 32
Appendix A. Report: A Brief Survey of Morphological Characteristics of
White-tailed Deer on Bald Head Island, North Carolina 33
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LIST OF TABLES
WHITE-TAILED DEER ON A BARRIER ISLAND: IMPLICATIONS FOR PRESERVING
AN ECOLOGICALLY IMPORTANT MARITIME FOREST
Table 1. Use-availability data and simultaneous confidence intervals using the Bonferroni
approach for habitat use type by female white-tailed deer (n = 11) on Bald Head
Island, North Carolina, 2008 – 2010 23
APPENDIX A
REPORT: MORPHOLOGY OF WHITE-TAILED DEER ON BALD HEAD ISLAND,
NORTH CAROLINA
Table 1. Morphological measurements of white-tailed deer sampled on Bald Head Island,
North Carolina from 2008-2009 37
1
Assessment of White-tailed Deer on Bald Head Island, North Carolina
Introduction:
White-tailed deer (Odocoileus virginianus) have the potential to negatively impact
forest systems, and in the absence of reproductive controls can negatively impact ecosystems
through over-browsing. Over the last decade, the public, the Village of Bald Head Island,
and the Bald Head Island Conservancy have become increasingly concerned with the density
of the white-tailed deer population on Bald Head Island, North Carolina. During the early
2000‟s, white-tailed deer density began to increase on Bald Head Island which prompted
concern regarding the potential impacts to the maritime forest, the predominant vegetative
community of this barrier island. Further, there was a lack of reproductive controls on the
white-tailed deer population as hunting was prohibited and there were no natural predators.
Hence, to provide managers with empirical data necessary to effectively manage the white-
tailed deer population and preserve the integrity of the maritime forest, I conducted research
on the white-tailed deer population on Bald Head Island.
From January 2008 to January 2010, I radiocollared 13 white-tailed deer to evaluate
emigration, home range, cover type use, and population density on Bald Head Island.
Emigration of white-tailed deer could potentially impact management decisions on
population control methods (i.e., annual culls, immunocontraception, etc.) implemented by
managers. Also, deer home range and cover type use could have implications for conserving
maritime forest if deer selectively use this forest over other available habitat. Higher
proportionate use of maritime forest, coupled with increased deer density, could negatively
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impact forest regeneration through over-browsing, thereby hindering the conservation of the
maritime forest ecosystem.
Additionally, Bald Head Island managers were interested in determining if white-
tailed deer had been exposed to diseases that could have potential health implications for
humans and pets on the island. Surveillance of wildlife disease can be an important
component in wildlife management if there is public concern over potential exposure risks to
wildlife related diseases. Therefore, I surveyed white-tailed deer on Bald Head Island for the
presence of select pathogens that have zoonotic potential. Whole blood samples were tested,
using polymerase chain reaction (PCR) methods, for Bartonella spp. and Borrelia
burgdorferi. Also, I tested serum samples for total antibodies to six different serovars of
Leptospira interrogans using a microscopic agglutination test (MAT). Serum samples were
tested for antibodies to Anaplasma phagocytophilum and Borrelia burgdorferi using a
polyvalent enzyme-linked assay (ELISA) or an indirect fluorescent antibody (IFA) staining
method.
Finally, I provided data on the morphological characteristics of captured white-tailed
deer for Bald Head Island managers. I collected measurements on white-tailed deer body
weight, total body length, body circumference, and hind foot length. This information could
prove useful in future studies of white-tailed deer on Bald Head Island, or in comparative
studies conducted in other localities.
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White-tailed Deer on a Barrier Island: Implications for Preserving an Ecologically
Important Maritime Forest
Brandon L. Sherrill, North Carolina State University, Department of Forestry and
Environmental Resources, Fisheries, Wildlife, and Conservation Biology Program,
Turner House, Box 7646 Raleigh, NC 27695-7646
Anthony G. Snider, University of North Carolina Wilmington, Department of Environmental
Studies, 601 S. College Rd., Wilmington, NC 28403
Christopher S. DePerno, North Carolina State University, Department of Forestry and
Environmental Resources, Fisheries, Wildlife, and Conservation Biology Program,
Turner House, Box 7646 Raleigh, NC 27695
Abstract:
In recent years, the white-tailed deer (Odocoileus virginianus) population on Bald Head
Island, North Carolina has increased, threatening a unique maritime forest in southeastern
North Carolina. Bald Head Island is ~620 ha and is characterized by live oak (Quercus
virginiana) maritime forest, dunes, tidal marsh, and urban development. Preservation of
maritime forest is important for barrier island conservation. Maritime forests are important
coastal habitats that are under significant threat from development, and in the absence of
reproductive controls, white-tailed deer can negatively impact ecosystems through over-
browsing. Therefore, our objectives were to determine emigration, home range, cover type
use and selection, and population density of white-tailed deer on Bald Head Island to provide
baseline information which could impact deer management decisions. From 5 January
through 31 March 2008 and 2 January through 31 January 2009, 12 females and one male
were chemically immobilized and equipped with VHF radiocollars. From January 2008
through January 2010, a minimum of four visual locations were obtained per animal per
month. We used a fixed kernel density estimator to calculate 90% (home range) and 50%
4
(core area) utilization contours for radiocollared female deer (n = 11). To determine cover
type use and selection, we used land cover data generated by the Southeast Gap Analysis
Project and a Chi-square ( 2) goodness-of fit test to determine differences between expected
and observed use of cover types within home ranges. Significance levels for 95% confidence
intervals were determined using the Bonferroni method. From May through August 2008
and 2009, spotlight surveys were conducted and used to generate population estimates using
Lincoln-Peterson index. No radiocollared white-tailed deer migrated from Bald Head Island
during the course of the study and average home range and core areas were 60.73 ha (SE =
5.63) and 15.00 ha (SE = 1.37), respectively. Maritime forest/shrub comprised ~275 ha
(44%) of available habitat on Bald Head Island and were used by radiocollared deer at levels
greater than available, whereas dune/grasslands were used less than available. All other
cover types were used in proportion to availability. Population densities of white-tailed deer
were 17 and 15 deer/km2 for 2008 and 2009, respectively. Based on home range size and
cover type selection, and until additional research is conducted, we recommend that white-
tailed deer populations be managed at current levels to prevent degradation of important
maritime forest habitat.
Key words: Bald Head Island, home range, live oak, maritime forest, Odocoileus
virginianus, Quercus virginiana, white-tailed deer
Proc. Annu. Conf. Southeast. Assoc. Fish and Wildl. Agencies : -
White-tailed deer (Odocoileus virginianus), in the absence of predators or other
reproductive controls, can negatively impact the growth rate and survival of tree seedlings
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and saplings, shrubs, and herbaceous plants through selective foraging, thereby altering plant
species diversity, structural heterogeneity, productivity, succession, and forest regeneration
(Huntly 1991, Russell et al. 2001, Horsley et al. 2003, Côté et al. 2004, Forrester et al. 2006).
Further, deer can reduce natural diversity of plant communities through monopolization of
resources, introduction and spread of disease, and by shifting relative abundance of plant
species and causing local extinctions (Temple 1990, Garrott 1993).
In recent years, the white-tailed deer population on Bald Head Island, North Carolina
has increased, threatening maritime live oak (Quercus virginiana) forest which is a relatively
rare and unique habitat, typically restricted to narrow areas along the inland coastline and
barrier islands (Wells 1939, Bourdeau and Oosting 1959, Bellis and Keough 1995). Also,
Bald Head Island represents the most northerly range of the cabbage palmetto (Sabal
palmetto) (Wells 1939). Natural disturbances inherent to maritime forests, combined with
increased urban development and recreational pressure, have contributed to the decline of
maritime forest (USFWS 1997, Forrester and Leopold 2006). On Bald Head Island, ~70 ha
of maritime forests are preserved through the North Carolina Coastal Reserve (North
Carolina Coastal Reserve 2010).
Often, white-tailed deer management is necessary to reduce the population and level
of impact on natural ecosystems and private property; however, management of deer
populations incites emotional and political conflict among individuals who want to reduce
deer population numbers (Diamond 1992, Diefenbach et al. 1997, Russell et al. 2001),
individuals who oppose hunting or culling deer (McShea and Rappole 1997, Russell et al.
2001), and land managers who distrust human intervention in "natural" processes within
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wildlife refuges and preserves (Diamond 1992). Staff from the Bald Head Island
Conservancy, a non-profit organization created to protect, preserve, and promote the natural
environment of the island, along with researchers from the University of North Carolina at
Wilmington, have hypothesized, based on anecdotal evidence and preliminary research, that
white-tailed deer negatively impact live oak recruitment on Bald Head Island (S. Dorsey,
Bald Head Island Conservancy, pers. commun.). Therefore, to limit the potential impact of
white-tailed deer on maritime forest, the Village of Bald Head (i.e., the governmental
administration) implemented population control measures to stabilize and possibly reduce
white-tailed deer density on the island. During 2003, 2005-2007, and 2009, culling was
conducted resulting in the removal of 559 individuals (average = 111.8, range = 71-149
deer/year). Due to increased social and political conflict over the public acceptability and
safety concerns of culling, management officials decided to evaluate immunocontraception, a
non-lethal control method, as an alternative to lethal control programs to manage the white-
tailed deer population. Effective implementation of an immunocontraception program
requires quantitative knowledge of the target population (i.e., population size, immigration,
emigration, etc.) to project the success of population control measures (Seagle and Close
1996). Migration is an important parameter to consider when using immunocontraceptives,
as it can have significant impacts on control of small populations (Seagle and Close 1996).
Therefore, our objectives were to determine emigration, home range, cover type use and
selection, and population density of white-tailed deer on Bald Head Island to provide
managers with baseline data on the population to facilitate more informed management
decisions and thereby potentially limit negative impacts to the maritime forest.
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STUDY AREA
Bald Head Island was located at the mouth of the Cape Fear River in Brunswick
County, North Carolina and was the largest of three relict beach ridges (Bald Head Island,
Middle Island, and Bluff Island) collectively referred to as the Smith Island Complex
(Cooper and Satterthwaite 1964). Bald Head Island was bounded on the south and east by
the Atlantic Ocean, the west by the Cape Fear River, and the north by tidal marsh. The
Smith Island Complex was connected to the mainland to the north by a narrow stretch of
beach due to the closing of inlets along the coastline between the island complex and Fort
Fisher. Bald Head Island, composed of approximately 620 ha of upland habitat, was ~5.6 km
long and ~1.2 km wide consisting of successive stages of maritime forest/shrub,
dune/grassland, tidal marsh, and urban development (Cooper and Satterthwaite 1964, Ray et
al. 2001). Maritime forest/shrub comprised ~275 ha (44%) of Bald Head Island and was
characterized by live oak, laurel oak (Quercus hemisphaerica), cabbage palmetto (Sabal
palmetto), redbay (Persea borbonia), Carolina laurelcherry (Prunus caroliniana), American
holly (Ilex opaca), yaupon (Ilex vomitoria), devilwood (Osmanthus americanus), loblolly
pine (Pinus taeda), red mulberry (Morus rubra), wax myrtle (Morella cerifera), eastern
redcedar (Juniperus virginiana), American beautyberry (Callicarpa americana), and dogwood
(Cornus florida) (Oosting 1954, Bourdeau and Oosting 1959, Cooper and Satterthwaite
1964). Dune/grassland, covered with seaoats (Uniola paniculata) and other salt-resistant
herbs, represented ~171 ha (28%) of available habitat and transitioned into open shrub zones
of eastern redcedar, wax myrtle and catbrier (Smilax auriculata) (Cooper and Satterthwaite
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1964, J. Taggart, University of North Carolina Wilmington, pers. commun.). Tidal marsh
consisted of saltmarsh cordgrass (Spartina alterniflora), black needlerush (Juncus
roemericanus), and a transitional fringe of saltgrass (Distichlis spicata), sea ox-eye (Borrichia
frutescens), and seacoast marshelder (Iva imbricate) and occupied the low saline soils
between Bald Head Island and the relict islands to the north (Cooper and Satterthwaite 1964,
J. Taggart, University of North Carolina Wilmington, pers. commun.). Developed areas
comprised ~85 ha (14%) of the available habitat on Bald Head Island. During the last
century, white-tailed deer were removed to control competition with livestock that once
occupied Bald Head Island, and were not reported in two comprehensive mammalian surveys
conducted in 1964 and 1970 (Ray et al. 2001). The current white-tailed deer population
likely immigrated to the island after development began in the mid-1980‟s (Ray et al. 2001).
METHODS
During January-March 2008 and January 2009, we captured white-tailed deer using a
CO2 powered dart rifle (Model JM Standard, Dan-Inject, Inc., Børkop, Denmark) and a
cartridge-fired dart rifle (Pneu-Dart, Williamsport, Pennsylvania, USA) to administer
anesthetic drug combinations of Telazol® (1:1 tiletamine hydrochloride and zolazepam
hydrochloride; Fort Dodge Animal Health, Fort Dodge, Iowa, USA) and XYLA-JECT®
(xylazine hydrocholoride, Phoenix Pharmaceutical, Inc., St. Joseph, Missouri, USA). We
immobilized darted deer with an intramuscular injection of 4.4 mg/kg of Telazol® and 2.2
mg/kg of xylazine hydrochloride (Kilpatrick and Spohr 1999, Kreeger et al. 2002).
Immobilizing drugs were administered with disposable, 2-cc wire-barbed darts equipped with
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radiotransmitters (Pneudart, Williamsport, Pennsylvania, USA). If a deer was not fully
chemically immobilized when located, we administered 2 mg/kg of KETASET® (ketamine
hydrocholride, Fort Dodge Animal Health, Fort Dodge, Iowa, USA) intramuscularly by
syringe.
Once immobilized, we applied eye ointment and a blindfold, and monitored body
temperature, respiration, pulse rate, and blood oxygen saturation. We excised the dart,
flushed the wound with Betadine® (povidone-iodine, Purdue Pharma, L.P., Stamford,
Connecticut, USA), and applied antibiotic cream (Neosporin®, Johnson & Johnson, Inc.,
New Brunswick, New Jersey, USA). Also, as a precautionary measure we administered a 3
ml subcutaneous injection of Bio-Mycin® 200, a broad spectrum antibiotic (oxytetracycline,
Boehringer Ingelheim Vetmedica, Inc., St. Joseph, Missouri, USA). We determined sex and
age and deer were classified as fawn (<1 yr old), yearling (≥1-<2 yr old), or adult (>2 yr old).
We placed a uniquely numbered cattle tag and piglet tag (National Band and Tag, Co.,
Newport, Kentucky, USA) in the right and left ears, respectively, and fitted each deer with a
mortality-sensing VHF radiocollar (TenXsys, Inc., Eagle, Idaho, USA). After processing
was complete, we intravenously administered yohimbine hydrochloride at 0.125 mg/kg
(YOBINE®; Wildlife Laboratories, Inc., Fort Collins, Colorado, USA). We monitored deer
until they were able to regain muscular control to stand and/or leave the processing site. The
research protocol was reviewed and approved by the Institutional Animal Care and Use
Committee at the University of North Carolina at Wilmington (#2007-017).
From January 2008 through January 2010, we visually located all radiocollared
deer a minimum of four times per month to obtain an adequate number of locations per
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individual (Seaman et al. 1999) for home range analysis using a 2-element antenna and
portable radio receiver (Telonics TR-4, Mesa, AZ, USA). Limited funding restricted our
ability to conduct research on the island (i.e., transportation, ferry travel, accommodations,
etc.) which impacted the number of locations we could obtain per individual. We conducted
radio telemetry only during diurnal time periods. Kernohan et al. (1996) failed to detect
differences between white-tailed deer home range estimates from diurnal and 24-hr habitat
use; therefore, we believe home range estimates from combined, diurnal and nocturnal,
telemetry locations would not differ from diurnal-only home range estimates and would
produce similar habitat use estimates. Further, we randomized the order in which we tracked
individuals during diurnal telemetry sessions to reduce temporal bias within our samples.
We recorded locations with a hand-held GPS unit, entered coordinates into ArcMap 9.3.1
(Environmental Systems Research Institute, Inc., Redlands, California, USA) and generated
home range and core area estimates with 90% and 50% utilization contours, respectively,
using „Fixed Kernel Density Estimator‟ and „Percent Volume Contour‟ in Hawth‟s Analysis
Tools (Seaman et al. 1999, Beyer 2004, Börger et al. 2006). We tested home range size for
normality using Lilliefor‟s test for normal distribution (Kilpatrick and Spohr 2000). We
compared home range size between years for deer with two years of telemetry data using a
paired t-test (P < 0.05). If home range size did not differ between years, we pooled all
locations from individual deer to calculate landscape measurements.
We used land cover data generated by the Southeast Gap Analysis Program (USGS
National Gap Analysis Program 2008) in ArcMAP to classify cover type use and availability
as open water, development, maritime forest/shrub, dune/grassland, and tidal marsh.
11
Estimated radiocollared deer cover type use was determined as the average of percent
coverage of cover types incorporated within home ranges for the entire study period. A Chi-
square ( 2) goodness-of fit test was used to determine differences between expected and
observed use of cover types within home ranges (Neu et al. 1974, Byers et al. 1984, Jelinski
1991). Significance levels for 95% confidence intervals were determined using the
Bonferroni method (Neu et al. 1974, Byers et al. 1984).
We conducted spotlight surveys over an established 10 km route from May through
September 2008 and 2009. We conducted surveys approximately one hour after sunset using
a golf cart traveling ~8 km/hour. We recorded the number deer seen and noted when marked
deer (i.e., radiocollared and ear tagged) were spotted. We calculated population estimates
using Lincoln-Peterson index [ , , ,
] via mark-resight data.
RESULTS
During this study, 13 [2008 (n = 8) and 2009 (n = 5)] white-tailed deer were captured.
In 2008, we captured one adult male along with one fawn, one yearling, and five adult
females. In 2009, we captured one fawn, one yearling, and three adult females. In 2008, the
radiocollar of the one male captured failed one week after deployment and in 2009, one
female deer was injured from a vehicle collision and euthanized two weeks after being
collared; neither deer were included in the analyses.
All radiocollared female deer (n = 11) were located on Bald Head Island or on small
hammocks (islands) in marshes between Bald Head and Middle Islands throughout the two
12
year survey period; no radiocollared deer emigrated from Bald Head Island to the mainland.
We collected an average of 70 locations (range = 23-89) per individual for home range
analysis. Mean 90% home range was 60.73 ha (SE = 5.63, range = 38-93 ha) and mean 50%
core area was 15.00 ha (SE = 1.37, range = 9-22 ha) for all monitored deer. No differences
were detected in annual home range size (t = 1.85, df = 6, P = 0.11) for deer with two years
of data, therefore, we pooled telemetry locations to estimate home range estimates and
landscape measurements. Maritime forest/shrub was used by radiocollared deer at levels
greater than available, whereas dune/grassland was used less than available (Table 1). Open
water, developed, and tidal marsh cover types were used in proportion to availability (Table
1).
In 2008, 30 spotlight surveys were conducted and we estimated the population at
106.5 (SE = 17.8, CI = ± 34.9) equating to ~17 deer/km2. In 2009, 34 surveys were
conducted and we estimated the population at 93.4 (SE = 27.8, CI = ± 54.5) equating to ~15
deer/km2.
DISCUSSION
In recent decades, deer populations in urban, suburban, and natural areas have
increased, and there is evidence of damage to forest vegetation, crops, and wildlife habitat
attributable to deer (Horsley et al. 2003). This increase has escalated the need for intensive
management of this species; however, social and political acceptability of lethal control
methods for wildlife populations often dictates the need for alternative, non-lethal, control
programs. Our research focused on deer home range and emigration to provide baseline data
13
to effectively manage deer using non-lethal methods. During this study, no radiocollared
deer emigrated from the Smith Island Complex as female deer often show site fidelity across
seasons and years (Beier and McCullough 1990). Home ranges of white-tailed deer on Bald
Head Island were confined to the island and the surrounding marsh and hammocks. Our
home range estimates for white-tailed deer were similar to those generated by studies
conducted on some suburban and exurban populations (Cornicelli et al. 1996, Kilpatrick and
Spohr 2000, Etter et al. 2002), larger than estimates from other urban and suburban
populations (Grund et al. 2002, Porter et al. 2004), but smaller than estimates from rural
populations (Tierson et al. 1985, Nixon et al. 1991, Campbell et al. 2004). Home range
estimates vary significantly by locality and analysis method; therefore, conclusions from
comparisons between studies should be made with caution. White-tailed deer could
immigrate to Bald Head Island from the mainland through the river and marshes located to
the west/northwest, or down the beach from the north; however, further research is necessary
to document movement of deer to Bald Head Island.
Barrier islands in the southeastern United States are usually considered to be low
quality habitat for white-tailed deer and even the best quality southern forest systems sustain
white-tailed deer densities of ~19 deer/km2 (Stransky 1969, Osborne et al. 1992); however,
some of these island habitats have supported densities as high as 40 deer/km2, despite low
deer reproductive rates, infertile soils, poor-quality forage, and high annual harvest (Osborne
et al. 1992). In 1999, spotlight surveys on Bald Head and Middle Islands indicated a deer
density of ~21 deer/km2
(Ray et al. 2001). However, during the mid-2000‟s, anecdotal
evidence (i.e., from Bald Head Island Conservancy staff and island residents) and data from
14
spotlight surveys conducted by other researchers indicated an increase in the white-tailed
deer population and by 2004 the deer density was ~80 deer/km2 (M. Dewire, Bald Head
Island Conservancy, pers. commun.). Concern over impacts of increased deer density led
Bald Head Island managers to implement annual deer culls in 2003, 2005-2007, and 2009 to
reduce the population. Interestingly, after several years of culling, our population estimates
from 2008-2009 indicated the white-tailed deer density was between 15-17 deer/km2,
suggesting that culling was effective in reducing the population.
Although we present Lincoln-Peterson estimates from spotlight surveys, these
estimates are simply an index of the population and spotlight surveys can have limited value
to managers for obtaining accurate estimates of abundance of white-tailed deer populations
(Rakestraw et al. 1998, Collier et al. 2007). McCullough and Hirth (1988) concluded that it
is difficult to derive accurate estimates of white-tailed deer by mark-resight methods; but the
methods are useful for monitoring trends in populations over time if biases are consistent.
We provided Bald Head island managers with population size estimates as an index by which
to gauge the temporal success of population control programs. Seagle and Close (1996)
suggested that simple population indices are acceptable for monitoring success of
management programs where intensive population management for a maximum sustainable
harvest is not a priority. Future estimates of white-tailed deer populations should account for
biases associated with this survey technique, and possibly incorporate additional techniques
(e.g., camera surveys, forward looking infrared, etc.).
Increased urban development on barrier islands, including Bald Head Island, has
significantly impacted maritime forests. Although white-tailed deer have been culled and a
15
preserve created to protect the maritime forest, increased browsing pressure from white-tailed
deer could prevent recruitment of live oak seedlings, thereby altering the vegetative structure
of this unique forest type. Our results revealed that female white-tailed deer selected
maritime forest/shrub at levels greater than available which could potentially impact forest
regeneration. Also, increased development on Bald Head Island could cause deer to use
maritime forest/shrub even more disproportionally, accelerating forest degradation.
Preservation of the maritime forest is important and should incorporate white-tailed
deer management, and account for urban development and the social carrying capacity of
deer on the island. To assess the ecological impact white-tailed deer have on the maritime
forest of Bald Head Island, future research must incorporate detailed vegetation studies and
diet analyses of white-tailed deer to determine the carrying capacity of the island. This
information, along with more precise estimates of population density will allow for sound
white-tailed deer management.
MANAGEMENT IMPLICATIONS
Although controversial, lethal control methods have been effective at maintaining the
deer population at a level that maintains the integrity of the maritime forest. The use of
immunocontraception has been proposed as an alternative means of population control on
Bald Head Island. For birth control methods to be effective, emigration of white-tailed deer
from Bald Head Island needs to be minimal. Our results indicated that radiocollared white-
tailed deer are year round residents on Bald Head Island; however, less is known about the
movement of white-tailed deer on the mainland. Our population estimates of white-tailed
16
deer densities are consistent with what barrier islands can sustain based on available research
(Stransky 1969, Osborne et al. 1992). At the current population densities, no data, or
anecdotal evidence, has been presented to suggest that deer are causing extensive damage to
the maritime forest (i.e., browse lines). Based on our research, white-tailed deer select
maritime/shrub over other available cover types which could potentially threaten this forest
system if deer density increases. Therefore, until further research is conducted, such as deer
diet analysis and vegetation surveys to quantify changes in structure and composition, we
recommend maintaining the deer population at current levels. Also, we recommend that
managers continue current population surveys and attempt to reduce confidence intervals
around population estimates. White-tailed deer management will depend on the Village of
Bald Head Island‟s objectives, the social carrying capacity of deer, deer density, and
available habitat. Integration of research and white-tailed deer management will be
necessary to ensure the integrity of the unique and fragile maritime forest is maintained.
ACKNOWLEDGMENTS
We would like to thank undergraduate and graduate students from North Carolina
State University and University of North Carolina at Wilmington that volunteered their time
to assist in data collection. Also, we thank Drs. M. Stoskopf and S. Kennedy-Stoskopf for
their consultation in the field and assistance in the lab, Dr. S. Dorsey and M. Dewire for their
assistance on Bald Head Island, and P. Gillikin for her assistance and knowledge in the field.
This study was funded by the Village of Bald Head Island, the Fisheries and Wildlife
Sciences Program at North Carolina State University, the Department of Environmental
17
Studies at the University of North Carolina at Wilmington, and the Bald Head Island
Conservancy. We thank M.C. Chitwood, S. Kennedy-Stoskopf, and H. Cheshire for
comments on previous drafts.
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23
Table 1: Use-availability data and simultaneous confidence intervals using the Bonferroni
approach for cover type use by female white-tailed deer (n = 11) on Bald Head Island, North
Carolina, 2008 – 2010.
Cover type
Total area
(ha)
Expected
proportion
of use
Actual
proportion
of use
Bonferroni
intervals for P
Open Water 6.6 0.011 0.009 -0.015 ≤ P ≤ 0.033
Developed 85.3 0.138 0.084 0.014 ≤ P ≤ 0.154
Maritime Forest/Shrub 276.3 0.445 0.668 0.550 ≤ P ≤ 0.790*
Dune/Grassland 177.1 0.285 0.113 0.034 ≤ P ≤ 0.192*
Tidal Marsh 74.7 0.121 0.126 0.043 ≤ P ≤ 0.210
Total 620.0 1.000 1.000
* Indicates a significant difference at the 0.05 level
24
Survey of Zoonotic Pathogens in White-tailed Deer on Bald Head Island, North
Carolina
Abstract:
White-tailed deer (Odocoileus virginianus) on Bald Head Island, North Carolina,
USA, a barrier island that has experienced steady urban development over the past several
decades, were screened for multiple zoonotic pathogens. Blood was collected from eight
deer in January through March 2008 and five deer in January 2009. We tested serum
samples for antibodies to Anaplasma phagocytophilum, Borrelia burgdorferi, and six
serovars of Leptospira interrogans, and whole blood samples for DNA from Bartonella spp.
and B. burgdorferi. Serum samples were screened using either a polyvalent enzyme-linked
immunosorbent assay (ELISA), an indirect fluorescent antibody (IFA) staining method, or a
microscopic agglutination test (MAT). Whole blood samples were screened using
conventional polymerase chain reaction (PCR) analysis. All sera were negative for L.
interrogans, two serum samples tested positive for A. phagocytophilum, and one was positive
for B. burgdorferi. Whole blood PCR results were negative for Bartonella spp. and B.
burgdorferi. Continued surveillance of wildlife disease is necessary to determine prevalence
of specific pathogens, their impacts on the white-tailed deer population, and the risk of
exposure to humans and pets on Bald Head Island.
Surveillance is an integral component to identify and manage zoonotic diseases
(Belant and Deese, 2010). Bald Head Island, North Carolina, USA (~33°51„N, ~77°59„W) is
an affluent golf course community with a relatively high density white-tailed deer
25
population. Residential development began during the 1980‟s, and by the early 2000‟s the
number white-tailed deer on the island increased to a level that required managers to
implement a population control program (i.e., annual culls) (Sherrill et al., In Press). As deer
density increased, concerns related to deer impacts to forested habitat and public health (i.e.,
risk of disease exposure to humans and pets) also increased; therefore, during January-March
2008 and January 2009, I captured white-tailed deer using a CO2 powered dart rifle (Model
JM Standard, Dan-Inject, Inc., Børkop, Denmark) or a cartridge-fired dart rifle (Pneu-Dart,
Williamsport, Pennsylvania, USA) to collect blood samples to test for the presence of select
pathogens. I immobilized deer with an intramuscular injection of 4.4 mg/kg of Telazol® (1:1
tiletamine hydrochloride and zolazepam hydrochloride; Fort Dodge Animal Health, Fort
Dodge, Iowa, USA) and 2.2 mg/kg of XYLA-JECT® (xylazine hydrocholoride, Phoenix
Pharmaceutical, Inc., St. Joseph, Missouri, USA) (Kreeger et al., 2002, Sherrill et al., In
Press). I collected blood samples via jugular venipuncture to obtain a minimum of 6 ml for
whole blood and 10 ml to be centrifuged for serum to analyze for presence of select
pathogens. Serum samples were centrifuged within 30 minutes after collection, and all
samples were frozen. Additionally, external parasite loads were evaluated and individuals
were assigned a qualitative health score (i.e., poor, fair. good, excellent) based on overall
physical condition. Parasite loads and health scores were evaluated simply to provide Bald
Head Island managers with a subjective assessment of the overall health of the white-tailed
deer population. The research protocol was reviewed and approved by the Institutional
Animal Care and Use Committee at the University of North Carolina at Wilmington (#2007-
017).
26
I sent serum to the Connecticut Agricultural Experiment Station to detect total
antibodies to strain 2591 and recombinant antigen VlsE (VlsE1-HIS) of Borrelia burgdorferi,
and separate recombinant protein (p) 44 antigen of Anaplasma phagocytophilum using a
polyvalent enzyme-linked immunosorbent assay (ELISA) (Magnarelli et al., 1999, 2004).
Also, indirect fluorescent antibody (IFA) staining methods were used to detect antibodies to
strain NCH-1 of A. phagocytophilum (Magnarelli et al., 1999). I sent serum samples to the
Michigan State University Diagnostic Center for Population and Animal Health to be tested
for agglutinating antibodies against Leptospira interrogans (serovars bratislava, canicola,
grippotyphosa, hardjo, icterohemorrhagica, and pomona) using a microscopic agglutination
test (MAT) (Cole et al., 1973). I sent whole blood samples to North Carolina State
University College of Veterinary Medicine to screen for Bartonella spp. (Diniz et al., 2007)
and B. burgdorferi (Maggi et al., In Press) using polymerase chain reaction (PCR) analyses.
During this study, 13 [2008 (n = 8) and 2009 (n = 5)] white-tailed deer were
chemically immobilized and radiocollared. In 2008, I captured one adult male along with
one fawn, one yearling, and five adult females. In 2009, I captured one fawn, one yearling,
and three adult females. All test results for Bartonella spp. and L. interrogans were negative.
One female was seropositive for the p44 recombinant A. phagocytophilum antigen with
antibody titers of 1:320. The male was seropositive for p44 recombinant antigen and strain
NCH-1 of A. phagocytophilum with antibody titers of 1:256 and 1:320, respectively. All
PCR results from whole blood samples were negative for B. burgdorferi; however, the male
serum sample positive for A. phagocytophilum was also positive for the VlsE-1 recombinant
B. burgdorferi antigen with antibody titers of 1:640. All antibody-positive and –negative
27
sera were retested to assess reproducibility of results. Further, qualitative health scores of all
chemically immobilized deer were evaluated as good (n = 2) or excellent (n = 11) and
parasite loads were low.
Human exposure to Lyme disease, human granulocytic ehrlichiosis (HGE), and other
zoonotic pathogens is a concern for residents in close proximity to high density deer
populations. Borrelia burgdorferi, the causative agent of Lyme disease (Frank et al., 1998),
and A. phagocytophilum, the agent of HGE (Walker and Dumler, 1996), have been reported
in regions where the black-legged tick (Ixodes scapularis) occurs, and white-tailed deer are
important hosts for motile stages of this tick (Magnarelli et al., 2004). Deer can serve as
reservoir hosts of infectious diseases, and as sentinels for human diseases; therefore,
epidemiologic surveillance can be useful in identifying potential exposure risks to zoonotic
diseases (Wolf et al., 2008).
Serological results for A. phagocytophilum and B. burgdorferi indicate the occurrence
of these pathogens on Bald Head Island. Although our sample size is relatively small, it
represents approximately 12-14% of the white-tailed deer population on Bald Head Island
(Sherrill et al., In Press). Future research should incorporate increased sampling and
investigate primary vectors of these pathogens to determine prevalence of disease on Bald
Head Island and provide a measure of relative risk of exposure to wildlife and humans. I
believe initial results from my analyses indicate there is the potential for human exposure to
these pathogens.
This project was funded by the Village of Bald Head Island, North Carolina State
University, and the University of North Carolina at Wilmington. I thank the numerous
28
undergraduate and graduate students from both universities who volunteered on this project.
In addition, I thank staff at the Bald Head Island Conservancy for their support.
LITERATURE CITED
Belant, J. L. and A. R. Deese. 2010. Importance of wildlife disease surveillance. Human
Wildlife Interactions 4:165-169.
Cole, J. R., Jr., C. R. Sulzer, and A. R. Pursell. 1973. Improved microtechnique for the
leptospiral microscopic agglutination test. Applied Microbiology 25:976-980.
Diniz, P. P. V. P, R. C. Maggi, D. S. Schwartz, M. B. Cadenas, J. M. Bradley, B. Hegarty,
and E. B. Breitschwerdt. 2007. Canine bartonellosis: serological and molecular
prevalence in Brazil and evidence of co-infection with Bartonella henselae and
Bartonella vinsonii subsp. berkhoffii. Veterinary Research 38: 697-710.
Frank, D. H., D. Fish, and F. H. Moy. 1998. Landscape features associated with Lyme
disease risk in a suburban residential environment. Landscape Ecology 13:27-36.
Kreeger, T.J., J.M. Arnemo, and J.P. Raath. 2002. Handbook of wildlife chemical
immobilization: international edition. Wildlife Pharmaceuticals, Fort Collins,
Colorado.
Maggi, R. G., S. Reichelt, M. Toliver, B. Engber. In Press. Borrelia species in Ixodes affinis
and Ixodes scapularis ticks collected from the Coastal Plain of North Carolina. Ticks
and Tick Borne Diseases.
Magnarelli, L. A., J. W. IJdo, K. C. Stafford III, and E. Fikrig. 1999. Infections of
granulocytic ehrlichiae and Borrelia burgdorferi in white-tailed deer in Connecticut.
29
Journal of Wildlife Diseases 35:266-274.
_____, _____, U. Ramakrishnan, D. W. Henderson, K. C. Stafford III, and E. Fikrig.
2004. Use of recombinant antigens of Borrelia burgdorferi and Anaplasma
phagocytophilum in enzyme-linked immunosorbent assays to detect antibodies in
white-tailed deer. Journal of Wildlife Diseases 40:249-258.
Sherrill, B. L., A. Snider, and C. S. DePerno. In Press. White-tailed deer on a barrier island:
Implications for preserving an ecologically important maritime forest. Proceedings of
the Annual Conference of the Southeastern Association of Fish and Wildlife
Agencies.
Walker, D. H., and J. S. Dumler. 1996. Emergence of the ehrlichiosis as human health
problems. Emerging Infectious Diseases 2:18-29.
Wolf, K. N., C. S. DePerno, J. A. Jenks, M. K. Stoskopf, S. Kennedy-Stoskopf, C. C.
Swanson, T. J. Brinkman, R. G. Osborn, and J. A. Tardiff. 2008. Selenium status and
antibodies to selected pathogens in white-tailed deer (Odocoileus virginianus) in
southern Minnesota. Journal of Wildlife Diseases 44:181-187.
30
Conclusions
Baseline information collected on white-tailed deer on Bald Head Island will allow
managers to more effectively manage the deer population. I determined that radiocollared
white-tailed deer remained resident on Bald Head Island through the duration of the sampling
period which could have implications for determining appropriate population control
methods. Additionally, white-tailed deer used maritime forest at a higher proportion than it is
available. If deer density continues to increase, there is the potential for negative impacts to
vegetation through over-browsing which could prove detrimental to conservation efforts in
maintaining the integrity of the maritime forest.
Exposure to zoonotic diseases is often a concern in areas where wildlife populations
are in close proximity to humans. On Bald Head Island, I sampled white-tailed deer for
several pathogens to determine if I could detect the presence of disease. Tests for Bartonella
spp. and Leptospira interrogans were negative for all samples. Two deer tested positive for
Anaplasma phagocytophilum and one tested positive for Borrelia burgdorferi. Given my
results, there is the potential for human, and pet, exposure to diseases related to white-tailed
deer. However, additional research is necessary to determine the actual prevalence of
diseases and their potential impacts to human health.
Future research should attempt to quantify the actual impacts white-tailed deer have
on the maritime forest. Vegetation studies within the forest should determine if white-tailed
deer browsing alters the diversity and abundance of species within the forest community.
Additionally, deer diet analyses should be conducted to determine if deer selectively forage
31
on specific plant species within the maritime forest. This could include microhistological
analysis of deer fecal samples or examination of rumen content to identify plant species that
were consumed. Also, managers should continue to monitor the density of the deer
population to determine the carrying capacity of the island, and to provide an index to gauge
the effectiveness of population control methods.
I encourage the managers of Bald Head Island to consider the information provided in
this thesis, along with information from future research, when determining management
options for controlling the white-tailed deer population. Public perception and opinion often
drive the decision-making process regarding the management of wildlife populations;
however, it is important to incorporate empirical data, obtained through scientific research, in
any decision making process. Managers will have to balance the natural and social carrying
capacity of white-tailed deer on Bald Head Island to effectively manage this population and
conserve the ecologically important maritime forest.
32
APPENDICES
33
Appendix A
Report: A Brief Survey of Morphological Characteristics of White-tailed Deer on Bald
Head Island, North Carolina
BACKGROUND
External white-tailed deer morphology can vary by geographic region and be affected
by genetics, food availability and population density (Wolverton et al. 2009). On Bald Head
Island, North Carolina I chemically immobilized white-tailed deer to estimate movement,
home range, cover type use, and to assess the presence of select pathogens. Additionally, I
collected several external measurements to provide baseline data on white-tailed deer
morphology.
Bald Head Island was located at the mouth of the Cape Fear River in Brunswick
County, North Carolina and was the largest of three relict beach ridges (Bald Head Island,
Middle Island, and Bluff Island) collectively referred to as the Smith Island Complex
(Cooper and Satterthwaite 1964). Bald Head Island was bounded on the south and east by
the Atlantic Ocean, the west by the Cape Fear River, and the north by tidal marsh. The
Smith Island Complex was connected to the mainland to the north by a narrow stretch of
beach due to the closing of inlets along the coastline between the island complex and Fort
Fisher. Bald Head Island, composed of approximately 620 ha of upland habitat, was 5.6 km
long and 1.2 km wide consisting of successive stages of maritime forest/shrub,
dune/grassland, tidal marsh, and urban development (Cooper and Satterthwaite 1964, Ray et
al. 2001).
34
METHODS
White-tailed deer were chemically immobilized (as described in Chapter 1) from
January-March 2008 and January 2009. Once immobilized, I applied eye ointment and a
blindfold, and monitored body temperature, respiration, pulse rate, and blood oxygen
saturation. I determined sex and age and deer were classified as fawn (<1 yr old), yearling
(≥1-<2 yr old), or adult (>2 yr old). I placed a uniquely numbered cattle tag and piglet tag
(National Band and Tag, Co., Newport, Kentucky, USA) in the right and left ears,
respectively, and fitted each deer with a mortality-sensing VHF radiocollar (TenXsys, Inc.,
Eagle, Idaho, USA).
I measured several morphological characteristics of captured white-tailed deer
including body weight, total body length (along the curve of the spine, from tip of snout to
base of tail), body circumference (at the sternum), and hind foot length (from point of hock to
tip of hoof). The research protocol was reviewed and approved by the Institutional Animal
Care and Use Committee at the University of North Carolina at Wilmington (#2007-017).
RESULTS
Measurements collected from immobilized white-tailed deer varied by individual
(Table 1). Body weight was not collected for one male and one adult female, but all other
morphological characteristics were measured for each individual. Average adult female body
weight, total body length, body circumference, and hind foot length were 39.8 kg (SE = 1.2),
122.6 cm (SE = 2.1), 84.5 cm (SE = 0.7), and 40.7 cm (SE = 0.3), respectively. Average
yearling female body weight, total body length, body circumference, and hind foot length
35
were 31.8 kg (SE = 5.5), 116.8 cm (SE = 9.8), 76.0 cm (SE = 4.6), and 39.2 cm (SE = 0.9),
respectively. Average fawn female body weight, total body length, body circumference, and
hind foot length were 26.6 kg (SE = 0.3), 117.0 cm (SE = 3.5), 73.8 cm (SE = 2.3), and 39.2
cm (SE = 0.3), respectively.
DISCUSSION
Bald Head Island provided a favorable location for a deer population study because
predation, automobile collisions, and emigration are minimal and hunting is absent. This
study provided useful baseline information of white-tailed deer on Bald Head Island, which
can be used in future research to observe changes in morphology on a temporal scale, or
compare insular populations to those in mainland habitats. Geographic distribution and
genetics can influence white-tailed deer morphology; genetically isolated large mammal
populations on islands are characteristically smaller than mainland populations, especially
when population density is high and food resources are over-exploited (Brisbin and Lenarz
1984). White-tailed deer density on Bald Head Island has been relatively high for the past
decade and mangers have implemented yearly culls to control the population level. Increased
deer density, and the impact to food resources, may be affecting deer morphology; however,
increased sampling over multiple years will be necessary to quantify changes in morphology
and to determine the contributing factors.
LITERATURE CITED
Brisbin, I.L., Jr., and M.S. Lenarz. 1984. Morphological comparisons of insular and mainland
36
populations of southeastern white-tailed deer. Journal of Mammalogy 65:44-50.
Cooper, A.W., and S. Satterthwaite. 1964. Smith Island and the Cape Fear Peninsula: a
comprehensive report on an outstanding natural area. Wildlife Preserves, Inc.,
Raleigh, North Carolina, USA.
Ray, D.K., E.G. Bolen, and W.M.D. Webster. 2001. Characteristics of a barrier island deer
population in the southeastern United States. The Journal of the Elisha Mitchell
Scientific Society 117:113-122.
Wolverton, S., M.A. Huston, J.H. Kennedy, and K. Cagle. 2009. Conformation to
Bergmann‟s rule in white-tailed deer can be explained by food availability. American
Midland Naturalist 162: 403-417.
37
Table 1: Morphological measurements of white-tailed deer sampled on Bald Head Island,
North Carolina from 2008-2009.
Sex Age Body
weight (kg) Total body length (cm)
Body circumference (cm)
Hind foot length (cm)
Male Adult - 143.5 108 46.5
Female Adult 40.4 122 85.5 41
Female Adult - 119.8 85 40.5
Female Adult 39.9 128.3 87.5 42.5
Female Adult 42.6 133 86 41.5
Female Adult 37.6 120.9 82.5 40.3
Female Adult 40.8 118 84.5 40.7
Female Adult 43.5 124.5 84 39.8
Female Adult 34 114 81 39.5
Female Yearling 26.3 107 71.4 38.3
Female Yearling 37.2 126.5 80.5 40
Female Fawn 26.3 113.5 76 39.5
Female Fawn 26.8 120.5 71.5 38.9